Sulfate radical-based oxidation of the antibiotics sulfamethoxazole, sulfisoxazole, sulfathiazole, and sulfamethizole: The role of five-membered heterocyclic rings
-
Add time:08/16/2019 Source:sciencedirect.com
The widespread occurrence of sulfonamides (SAs) in natural waters, wastewater, soil and sediment has raised increasing concerns about their potential risks to human health and ecological systems. Sulfate radical (SO4−)-based advanced oxidation processes (SR-AOPs) have become promising technologies to remove such contaminants in the environment. The present study systematically investigated the degradation of four selected SAs with different five-membered heterocyclic rings, namely, sulfamethoxazole (SMX), sulfisoxazole (SIX), sulfathiazole (STZ), and sulfamethizole (SMT), by thermo-activated persulfate (PS) process, and the role of heterocyclic rings was assessed particularly. The results revealed that all the selected SAs could be degraded efficiently by thermo-activated PS process, the decay rates of four SAs were appreciably increased with increasing temperature. For instance, degradation rates of STZ increased from 0.3 × 10−3 to 19.5 × 10−3 min−1 as the temperature was increased from 30 to 60 °C. Under the same experimental conditions, degradation rates of four SAs followed the order of SIX > SMX ≈ STZ > SMT, which is in accordance with decay rates of their R-NH2 moieties. The kinetic results indicated that five-membered heterocyclic rings could serve as reactive moieties toward SO4− attack, which were confirmed by frontier electron density (FED) calculations. Based on the transformation products identified by high-resolution mass spectrometry (HR-MS), five different oxidation pathways, including hydroxylation, aniline moiety oxidation, dimerization, sulfonamide bond cleavage, and heterocyclic ring oxidation/cleavage were proposed. Moreover, the degradation efficiency in real surface water (RSW) was found to be slight slower than that in artificial surface water (ASW), suggesting that SR-AOPs could be an efficient approach for the remediation of soil and water contaminated by these SAs.
We also recommend Trading Suppliers and Manufacturers of SulfaMethoxazole Related CoMpound F (cas 17103-52-5). Pls Click Website Link as below: cas 17103-52-5 suppliers
Prev:Degradation of sulfamethoxazole using ozone and chlorine dioxide - Compound-specific stable isotope analysis, transformation product analysis and mechanistic aspects
Next:Sediment and salinity effects on the bioaccumulation of sulfamethoxazole in zebrafish (Danio rerio)) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Full length articlePhotoelectrocatalytic degradation of sulfamethoxazole on g-C3N4/BiOI/EG p-n heterojunction photoanode under visible light irradiation08/20/2019
- Catalytic degradation of sulfamethoxazole through peroxymonosulfate activated with expanded graphite loaded CoFe2O4 particles08/19/2019
- Research paperSynthetic clay mineral as nanocarrier of sulfamethoxazole and trimethoprim08/18/2019
- Sediment and salinity effects on the bioaccumulation of sulfamethoxazole in zebrafish (Danio rerio)08/17/2019
- Degradation of sulfamethoxazole using ozone and chlorine dioxide - Compound-specific stable isotope analysis, transformation product analysis and mechanistic aspects08/15/2019
- Comprehensive study of sulfamethoxazole effects in marine mussels: Bioconcentration, enzymatic activities and metabolomics08/14/2019
- Metabolism of sulfamethoxazole in Arabidopsis thaliana cells and cucumber seedlings☆08/13/2019
- Research paperSynthesis of sulfamethoxazole and sulfabenzamide metal complexes; evaluation of their antibacterial activity08/12/2019


